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- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion type Assertion NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_head.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion wasGeneratedBy ECO_0000203 NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion wasDerivedFrom befree-2016 NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion SIO_000772 17646576 NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion evidence source_evidence_literature NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.
- NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_assertion description "[We describe an inherited, autosomal-dominant form of sinus node dysfunction caused by a missense mutation in the HCN4 ion channel pore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621329.RA6hFjmKJ-KkB-gQhkZTdQXIO4CqeqjP84SaMg8nxcuLA130_provenance.